(4-(N-(3-Chlorophenyl)sulfamoyl)phenyl)boronic acid

95%

Reagent Code: #215767
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CAS Number 957062-69-0

science Other reagents with same CAS 957062-69-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.55 g/mol
Formula C₁₂H₁₁BClNO₄S
badge Registry Numbers
MDL Number MFCD09878339
thermostat Physical Properties
Boiling Point 516.9±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.51±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides under palladium catalysis. The sulfonamide moiety enhances solubility and can participate in hydrogen bonding, making it useful in the development of bioactive molecules. Commonly employed in medicinal chemistry for constructing drug candidates targeting enzymes and receptors. Also applied in materials science for creating conjugated organic frameworks with tailored electronic properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,330.00
5g
10-20 days ฿6,980.00
(4-(N-(3-Chlorophenyl)sulfamoyl)phenyl)boronic acid
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Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides under palladium catalysis. The sulfonamide moiety enhances solubility and can participate in hydrogen bonding, making it useful in the development of bioactive molecules. Commonly employed in medicinal chemistry for constructing drug candidates targeting enzymes and receptors. Also applied in materials science for creating conjugated organic frameworks with tailored electronic properties.
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